Smith & Nephew logo

Senior Manufacturing Engineer - CMO

As a Senior Manufacturing Engineer - CMO, you will lead strategic initiatives and projects to enhance the Advanced Wound Management portfolio. You will manage complex changes, collaborate with cross-functional teams and external partners, and ensure regulatory compliance and quality. The role involves developing and implementing key projects to drive product sustainment and value creation, while also providing engineering support to key suppliers and maintaining manufacturing resilience.

Smith & Nephew United Kingdom
Hybrid Permanent
Smith & Nephew logo

Commercial Operations Specialist

Life. Unlimited. At Smith+Nephew we design and manufacture technology that takes the limits off living.Join our UK, Ireland and Nordics Commercial Centre of Excellence and play a key role in keeping critical commercial activity moving at S+N. This12 month fixed...

Smith & Nephew Watford, United Kingdom
Medtronic logo

Senior Territory Manager - Spine

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.A Day in the LifeThe...

Medtronic United Kingdom
OrganOx logo

Mechanical Design Engineer, Consumables

The Mechanical Design Engineer, Consumables role involves hands-on design, development, and verification of next-generation class III consumable perfusion sets. You will work within a cross-functional R&D team, collaborating with internal and external stakeholders to ensure high-quality product delivery and compliance with regulatory standards.

OrganOx Oxford, United Kingdom
On-site Permanent
OrganOx logo

Senior Supplier Assurance Engineer

The Senior Supplier Assurance Engineer leads supplier quality activities, ensuring compliance with global regulations and internal QMS processes. Key responsibilities include supplier qualification, performance monitoring, and continuous improvement, with a focus on maintaining high-quality standards across the supply chain.

OrganOx Oxford, United Kingdom
On-site Permanent Flexible
Medtronic logo

Upstream Product Manager

The Upstream Product Manager will lead the strategy and early-stage development of AI-enabled and edge-based software solutions for the Touch Surgery ecosystem. Responsibilities include defining product vision, conducting market research, partnering with engineering teams, and developing go-to-market strategies. The role requires deep expertise in AI, edge computing, and software marketing.

Medtronic London, United Kingdom
On-site Permanent
Newton Colmore logo

Mechanical Engineer - Programme Manager - Drug Delivery Devices

Mechanical Engineer - Programme Manager - Drug Delivery DevicesA period of significant growth has created an opportunity for a Programme Manager with a strong Mechanical Engineering background and deep, hands‑on experience in drug delivery device development. Based in Cambridge, you...

Newton Colmore Cambridge, United Kingdom
Permanent

Import/Export Operations Specialist

The Import/Export Operations Specialist ensures the compliant and efficient movement of medical devices across international borders. Responsibilities include managing customs processes, preparing trade documentation, and coordinating with freight forwarders and internal stakeholders to resolve shipment issues and maintain regulatory compliance.

Johnson & Johnson MedTech Leeds, United Kingdom
On-site Permanent

Manager, Clinical Research Med Affairs

The Manager, Clinical Research Med Affairs role involves providing strategic compliance leadership and practical guidance on clinical trials, investigator interactions, and scientific exchange. The role partners with global R&D, clinical research, and medical affairs teams to identify and mitigate compliance risks, ensuring ethical innovation and sound decision-making.

Johnson & Johnson MedTech Leeds, United Kingdom
On-site Permanent

Regulatory Affairs Specialist

The Regulatory Affairs Specialist will support the Quality & Regulatory team in maintaining and executing regulatory activities across a diverse product portfolio. Responsibilities include preparing technical documentation, ensuring compliance with global regulatory requirements, and coordinating audits. The role offers hands-on experience across the full product lifecycle and involves close collaboration with internal teams.

Cure Talent Uxbridge South, London, United Kingdom £40,000 – £50,000 pa
On-site Permanent

Product Development Scientist

The Product Development Scientist will work on the development and improvement of diagnostic products, from feasibility to launch, ensuring compliance with quality standards. Responsibilities include participating in product development phases, troubleshooting issues, and collaborating on technical analysis and documentation.

Right Match Recruitment Group Limited Dartford, Kent, United Kingdom £30,000 – £32,000 pa
Newton Colmore logo

Regulatory Affairs Specialist - Medical Devices - Cambridge

This role involves providing regulatory guidance across the full product development lifecycle, supporting multidisciplinary teams in a technology-driven environment. You will interpret global regulations including ISO 13485, ISO 9001, and FDA 21 CFR 820, ensuring compliance while enabling innovation. The position is embedded in project work, offering real-time input on regulatory strategy and contributing to quality management systems across medical and non-medical sectors.

Newton Colmore Cambridge, United Kingdom
Hybrid Permanent

Senior QA Validation Engineer

This role involves leading software verification and validation for safety-critical systems in a regulated environment, with a focus on test automation, regulatory compliance, and end-to-end traceability. The engineer will design test strategies, develop automated frameworks, and ensure alignment with quality standards across the development lifecycle. Collaboration with cross-functional teams is essential to resolve quality issues and support audits or regulatory submissions.

SoCode Impington, Cambridgeshire, United Kingdom £80,000 – £100,000 pa
On-site Permanent

Lead Manufacturing Engineer - NPI

The Lead Manufacturing Engineer will take ownership of manufacturing development activities, from early concept through to prototype and low-volume production. You will help define manufacturing strategy, assembly processes, tooling, and automation solutions, working closely with design engineers and external suppliers to transition products from R&D to commercial-ready production.

Redline Group Headington, Oxfordshire, United Kingdom £60,000 – £70,000 pa
On-site Permanent

Instrument Support Engineer (Hands-on R&D)

The role involves hands-on troubleshooting, assembly, and maintenance of cutting-edge laboratory instruments. You will collaborate closely with R&D and application support teams, manage projects independently, and work in a supportive, flexible environment.

HCL International London, United Kingdom £30,000 – £40,000 pa
Hybrid Permanent Flexible